WO2003092099A1 - Complex lithium metal oxides with enhanced cycle life and safety and a process for preparation thereof - Google Patents

Complex lithium metal oxides with enhanced cycle life and safety and a process for preparation thereof Download PDF

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Publication number
WO2003092099A1
WO2003092099A1 PCT/KR2003/000815 KR0300815W WO03092099A1 WO 2003092099 A1 WO2003092099 A1 WO 2003092099A1 KR 0300815 W KR0300815 W KR 0300815W WO 03092099 A1 WO03092099 A1 WO 03092099A1
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Prior art keywords
complex lithium
lithium metal
metal oxides
coating layer
oxides
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PCT/KR2003/000815
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English (en)
French (fr)
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Hong-Kyu Park
Yong Hoon Kwon
Seong Yong Park
Jin On Kim
Ki Young Lee
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Lg Chem. Ltd.
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Priority to AU2003222488A priority Critical patent/AU2003222488A1/en
Priority to EP03717762A priority patent/EP1497876B1/de
Priority to JP2004500352A priority patent/JP4465264B2/ja
Priority to US10/487,861 priority patent/US7235193B2/en
Publication of WO2003092099A1 publication Critical patent/WO2003092099A1/en

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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G51/00—Compounds of cobalt
    • C01G51/40—Cobaltates
    • C01G51/42—Cobaltates containing alkali metals, e.g. LiCoO2
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G51/00—Compounds of cobalt
    • C01G51/40—Cobaltates
    • C01G51/42—Cobaltates containing alkali metals, e.g. LiCoO2
    • C01G51/44—Cobaltates containing alkali metals, e.g. LiCoO2 containing manganese
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G53/00—Compounds of nickel
    • C01G53/40—Nickelates
    • C01G53/42—Nickelates containing alkali metals, e.g. LiNiO2
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G53/00—Compounds of nickel
    • C01G53/40—Nickelates
    • C01G53/42—Nickelates containing alkali metals, e.g. LiNiO2
    • C01G53/44—Nickelates containing alkali metals, e.g. LiNiO2 containing manganese
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/04—Processes of manufacture in general
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/139—Processes of manufacture
    • H01M4/1391—Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/362—Composites
    • H01M4/366—Composites as layered products
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/02—Amorphous compounds
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/50—Solid solutions
    • C01P2002/52—Solid solutions containing elements as dopants
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/50—Solid solutions
    • C01P2002/52—Solid solutions containing elements as dopants
    • C01P2002/54—Solid solutions containing elements as dopants one element only
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
    • C01P2002/88—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by thermal analysis data, e.g. TGA, DTA, DSC
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
    • C01P2004/82—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases
    • C01P2004/84—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases one phase coated with the other
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/40—Electric properties
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
    • Y10T428/2991—Coated

Definitions

  • the present invention relates to cathode active materials for lithium or lithium ion secondary batteries and a method for preparation thereof.
  • the present invention relates to a cathode active material that enhances high temperature storage properties, cycle life, and safety of the battery by forming an outer layer with amorphous complex lithium cobalt oxides on the surface of complex lithium metal oxides, which are used as the cathode active material, and a method for preparing the same cathode active material.
  • LiNiO 2 has the highest discharge capacity, problems arise in applying this material to practical use due to difficulties in synthesis and thermal safety. LiMn 2 O 4 is relatively low in price and does not harm the environment, but cannot be used alone, since it has a small specific capacity. LiCoO 2 has been used commercially for it has a high battery voltage and excellent electrode characteristics. However, it has poor storage properties at high temperatures. In order to resolve these problems, much research has been performed. According to Japanese Unexamined Patent Publication No. Hei 11-317230, the cycle life and safety of a battery have been enhanced by a metal oxide coating. In the LiNiO system, structural safety is improved by use of several dopants. In addition, safety of the battery is improved by improving thermal safety. Safety and cycle life of the battery are also improved by adding an additive to an electrolyte. However, such improvements do not affect storage properties and cycle life at high temperatures.
  • the present invention resolves the problems, which have been raised with respect to cycle life, safety and storage properties of a battery when a cathode active material is subject to room temperature and high temperatures.
  • the present invention provides a cathode active material that improves cycle life, safety and high temperature storage properties of a lithium ion secondary battery.
  • the present invention improves structural safety and electrochemical characteristics of the battery by forming a coating layer on the cathode active material with amorphous complex lithium cobalt oxides.
  • Fig. 1 is a graph showing charge and discharge characteristics of complex lithium cobalt oxides that form an amorphous coating layer on a core particle LiCoO 2 .
  • the outer coating layer in the prior art deteriorated in capacity, since it did not contain lithium.
  • the present invention prevents such capacity deterioration occurring after coating, by forming amorphous complex lithium metal oxides on the outer layer.
  • the amorphous lithium metal oxides have reversible capacity.
  • Fig. 2 is a graph showing discharge curves in their cycles. IR drop of the discharge curves in their cycles is significantly reduced.
  • Fig. 3 is a graph showing the results of the analysis of a calorific value of the complex lithium cobalt oxides performed by use of a Differential Scanning Calorimeter (DSC).
  • the calorific value is based on the temperature of complex lithium cobalt oxides obtained by decomposing a battery after charging the battery up to 4.2N When coating was performed, the initial temperature upon heat generation was increased and the calorific value was decreased. Therefore, it is possible to improve safety of the battery by inhibiting ignition of the battery, which is caused by heat generation at the cathode.
  • the present invention relates to a method of reforming a surface by forming a coating layer on the surface of complex lithium metal oxides in order to achieve the above-mentioned object.
  • This method for the preparation of the metal oxides comprises the following steps:
  • the present invention provides a lithium or lithium ion secondary battery that uses complex lithium metal oxides prepared by the above method as a cathode active material.
  • the present invention relates to obtaining a cathode active material that comprises core particles capable of absorbing, storing and emitting lithium ions, and a coating layer made of amorphous complex lithium metal oxides, which have low electric conductivity, and thus have low reactivity with an electrolyte.
  • Complex lithium metal oxides which have a voltage of 3. ON or more for lithium, or complex lithium cobalt oxides (LiCoO ) are used as core particles.
  • the coating layer is amorphous oxides comprising lithium cobalt oxides of formula Li ⁇ + x C ⁇ _ x _ y A y O , wherein 0 ⁇ x ⁇ 0.1, and 0 ⁇ y ⁇ 0.5.
  • A is selected from at least one of Al, B, Mg, Ca, Sr, Ba, ⁇ a, Cr, Gd, Ga, ⁇ i, Co, Fe, N Cr, Ti, Sn, Mn, Zr and Zn.
  • the method for coating the surface of complex lithium metal oxides, which are the core particle, with amorphous complex lithium cobalt oxides can be carried out as follows.
  • a homogeneously mixed solution is prepared by mixing the compounds, which will be used as raw material for forming amorphous complex lithium cobalt oxides, in a desired compositional ratio.
  • at least one of carbonate, nitrate, oxalate, sulfate, acetate, citrate, chloride, hydroxide, and oxide of the above metallic element or a mixture thereof can be used as raw material for forming the coating layer.
  • an organic solvent such as alcohol or a water-soluble solvent is preferably used to prepare a homogeneous mixture.
  • the amount of the coating layer ranges between 0.01-10 mol % based on the core particles, assuming that the mixture for forming the coating layer is oxidized after thermal treatment.
  • This coating method produces a slurry by adding a powder of complex lithium metal oxides, which are core particles, to a suspension (sol) of an organic solution or an aqueous solution of the compounds used as raw material for forming amorphous complex lithium cobalt oxides. By applying heat to the slurry during stirring by a stirrer, the compounds for forming amorphous complex lithium cobalt oxides are coated on the surface of the powder of complex lithium metal oxides during vaporization of the solvent.
  • amorphous complex lithium cobalt oxides are formed on the surface.
  • the flow rate of the gas ranges between 0.05-2.0 i /g*h (volume per weight and hour).
  • the heat treatment can be carried out for 0.1-10 hours, and most preferably 1-5 hours. The period of time and temperature for the heat treatment can be adjusted within the above-mentioned ranges depending on the situation.
  • a portion of the surface layer can be crystallized depending on the temperature of the heat treatment, and some elements may be doped on the surface of the core particle during the heat treatment.
  • a suspension of an aqueous solution or an organic solution, in which a mixture of feedstocks for forming amorphous complex lithium cobalt oxides is dissolved is sprayed on the surface of the core particles made of complex lithium metal oxides, and then dried to form a coating.
  • the suspension of a mixed solution is sprayed to form the coating.
  • the coating is dried by adjusting the temperature of the flowing air.
  • Dip coating is a more simplified coating method, in which complex lithium metal oxides (i.e., the core particles) are kept in a suspension of an organic solution or an aqueous solution in which dissolved feedstocks for forming amorphous complex lithium cobalt oxides during a predetermined time of period, are dried and coated.
  • complex lithium metal oxides coated with amorphous complex lithium metal oxides are obtained.
  • Li 2 CO 3 as a lithium feedstock and Co 3 O 4 as a cobalt feedstock were weighed in the molar equivalence ratio of Li: Co of 1.02: 1. Ethanol was added thereto as a solvent.
  • Li 2 CO 3 and Co 3 O 4 were ground together for 12 hours to be homogenized and then mixed.
  • the mixture was dried for 12 hours in a dryer, and calcinated for 10 hours at 400 ° C .
  • the mixture was ground and mixed again, and subjected to heat treatment for 10 hours at 900 °C .
  • the core particles LiCoO 2 were obtained.
  • the obtained core particles were coated with amorphous complex lithium cobalt oxides in the following manner.
  • Li when forming an amorphous coating layer
  • Co Co(CH 2 CO 2 ) 2 *4H 2 O was used.
  • the amount was adjusted in the equivalence ratio of 1.0:1.0.
  • the above feedstocks were dissolved in the ethanol, and stirred for 30 minutes to form a mixture solution containing homogeneous metallic compounds.
  • the amount of the mixture to be formed into a coating layer was adjusted to be 1 mol % for the core particles, assuming that all of the mixture is oxidized after heat treatment.
  • the slurry was coated on an aluminum foil.
  • the ⁇ MP solvent was vaporized and the foil coated with the slurry was dried.
  • a pressure of 500 kg/cm 2 was applied to the dried electrode. Then, the electrode was compressed and cut into cells.
  • a solution used as an electrolyte contains 1 mole of LiPF 6 dissolved in a solvent containing ethylene carbonate (EC) and ethylmethyl carbonate (EMC) in the ratio of 1 :2 by volume.
  • a half cell is prepared, wherein an electrode prepared in order to measure the cycle life and the high-rate discharge (C-rate) is a cathode, and a lithium metal is used as an anode.
  • the voltage for charge and discharge ranges from 3 to 4.2N
  • the cell was charged and discharged at 0.2C.
  • the high-rate discharge the cell was charged and discharged several times at 0.2C. Then, the capacities of 0.1C, 0.2C, 0.5C, 1C and 2C were measured.
  • Thermal safety of electrode active materials was tested at a rate of 0.5 min by use of the DSC by applying an electrolyte to a cathode that was obtained by charging it to 4.2N and then decomposing the battery. The above process was performed in a glove box in order to avoid any contact with air.
  • Li 2 CO 3 and Co(OH) 3 (lithium and cobalt feedstocks, respectively), and Al(OH) 3 to dope Al were used. At this time, they were weighed in the molar equivalence ratio of Li: Co: Al of 1.02:0.95:0.05. Then, these were mixed by adding ethanol as a solvent. By use of a ball mill, the mixture was ground together for 12 hours to be homogenized and then mixed. The mixture was dried for 12 hours in a drier, plasticized for 10 hours at 400 °C, and was ground and mixed again. Then, the mixture was subjected to heat treatment for 10 hours at 900 ° C to give a core particle made of LiCoo.g 5 Alo. 0 5O 2 . The other conditions were the same as in Example 1.
  • Example 1 The complex lithium cobalt oxides obtained in Example 1 were used as core particles.
  • Li 2 SO was used as the raw material of Li
  • Co(CH 3 CO 2 ) 2 -4H 2 O was used as the raw material of Co.
  • the amount was adjusted to be in the molar equivalence ratio of 1.02:1.0.
  • the process for forming the coating layer and the analysis of the characteristics thereof were performed under the same conditions as in Example 1.
  • the complex lithium cobalt oxides obtained in Example 1 were used as core particles.
  • LiCH 3 CO 2 *2H 2 ⁇ was used as the raw material of Li.
  • Al(CH 3 CO 2 ) 3 was used as the raw material of Al, and Co(CH 3 CO 2 ) 2*4H 2 O was used as the raw material of Co.
  • the amount was adjusted in the molar equivalence ratio of Li:Co:Al of 1.02.0.95:0.05.
  • the process for forming the coating layer and the analysis of the characteristics thereof were performed under the same conditions as in Example 1.
  • Example 1 The complex lithium cobalt oxides obtained in Example 1 were used as core particles.
  • LiCH 3 CO 2 *2H 2 O was used as the raw material of Li.
  • Al(CH 3 CO2) 3 was used as the raw material of Al, and Co(CH 3 CO 2 ) 2*4H 2 O was used as the raw material of Co.
  • the amount was adjusted to be in the molar equivalence ratio of Li:Co:Al of 1.02:0.9:0.1.
  • the process for forming the coating layer and the analysis of the characteristics thereof were performed under the same conditions as in Example 1.
  • Example 1 was repeated, except that complex lithium cobalt oxides (LiCoO 2 :C- 10H, Japan Chem.) were used.
  • Example 1 was repeated, except that the amount of the coating layer had a molar ratio of 5 mol % for the core particles.
  • Example 1 was repeated, except that complex lithium cobalt oxides (LiCoO 2 :C- 10H, Japan Chem.) were used as the core particles, and that the core particles, which were coated with a coating layer having the same composition as that of Example 1, were subject to heat treatment in air for 3 hours at 500 ° C . Comparative Example 1
  • Example 1 was repeated without coating the core particle obtained in Example
  • Example 1 was repeated without coating the core particle obtained in Example
  • Table 1 shows that the coated core particle is superior to those that are not coated with respect to the cycle life.
  • Table 2 shows that the coated surface is superior in high-rate discharge.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
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  • Inorganic Compounds Of Heavy Metals (AREA)
PCT/KR2003/000815 2002-04-23 2003-04-22 Complex lithium metal oxides with enhanced cycle life and safety and a process for preparation thereof WO2003092099A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
AU2003222488A AU2003222488A1 (en) 2002-04-23 2003-04-22 Complex lithium metal oxides with enhanced cycle life and safety and a process for preparation thereof
EP03717762A EP1497876B1 (de) 2002-04-23 2003-04-22 Komplexe lithiummetalloxide mit verbesserter zykluslebensdauer und sicherheit und prozess zu ihrer herstellung
JP2004500352A JP4465264B2 (ja) 2002-04-23 2003-04-22 寿命特性と安全性に優れたリチウム金属複合酸化物およびその製造方法
US10/487,861 US7235193B2 (en) 2002-04-23 2003-04-22 Complex lithium metal oxides with enhanced cycle life and safety and a process for preparation thereof

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KR1020020022167A KR20030083476A (ko) 2002-04-23 2002-04-23 수명 특성과 안전성이 우수한 리튬 금속 복합 산화물 및이의 제조 방법
KR10-2002-0022167 2002-04-23

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EP (1) EP1497876B1 (de)
JP (1) JP4465264B2 (de)
KR (1) KR20030083476A (de)
CN (1) CN1565063A (de)
AU (1) AU2003222488A1 (de)
WO (1) WO2003092099A1 (de)

Cited By (13)

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JP2006092820A (ja) * 2004-09-22 2006-04-06 Sanyo Electric Co Ltd 非水電解液二次電池用正極活物質及び正極並びに非水電解液二次電池
WO2007108610A1 (en) 2006-03-20 2007-09-27 Lg Chem, Ltd. Stoichiometric lithium cobalt oxide and method for preparation of the same
WO2008091707A2 (en) * 2007-01-25 2008-07-31 Massachusetts Institute Of Technology Oxide coatings on lithium oxide particles
EP1972018A2 (de) 2005-12-02 2008-09-24 A123 Systems, Inc. Amorphe und teilweise amorphe ionenspeichermaterialien auf nanomassstab
JP2008539536A (ja) * 2005-04-28 2008-11-13 比▲亜▼迪股▲分▼有限公司 電池正極及びこの電池正極を採用したリチウムイオン電池、並びにそれらの製造方法
EP2005503A1 (de) * 2006-03-20 2008-12-24 LG Chem, Ltd. Katodenmaterialien für eine lithiumbatterie mit höherer leistungsfähigkeit
US7656125B2 (en) 2005-07-14 2010-02-02 Boston-Power, Inc. Method and device for controlling a storage voltage of a battery pack
US7811708B2 (en) 2004-12-28 2010-10-12 Boston-Power, Inc. Lithium-ion secondary battery
US8138726B2 (en) 2006-06-28 2012-03-20 Boston-Power, Inc. Electronics with multiple charge rate
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